4.7 Review

Recent advances in asymmetric synthesis of 2-substituted indoline derivatives

Journal

CHINESE CHEMICAL LETTERS
Volume 31, Issue 2, Pages 311-323

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.cclet.2019.07.015

Keywords

Indolines; Asymmetric synthesis; Enantioselectivity; Nitrogen heterocycles; Synthetic methods

Funding

  1. National Natural Science Foundation of China [21702121, 91856119, 21622201]
  2. Science and Technology Department of Hubei Province [2016CFA050, 2017AHB047]
  3. Program of Introducing Talents of Discipline to Universities of China (111 Program) [B17019]

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Enantiomerically pure 2-substituted indolines are an important class of nitrogen heterocycles that occur frequently in many alkaloid natural products and biologically active compounds. Consequently, the synthesis of such skeletons is of great significance. The past years have witnessed a number of remarkable advances in the development of efficient strategies to construct this class of chiral compounds. This review summarizes the recent advances in asymmetric synthesis of 2-substituted indoline derivatives. Due to the limitation of the length, this review only summarizes those works published from January of 2012 to January of 2019. Meanwhile, methods towards synthesis of fused and spirocyclic indolines will not be discussed in this review. (C) 2019 Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences. Published by Elsevier B.V. All rights reserved.

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